ES2201635T3 - Co-formulacion fungicida. - Google Patents
Co-formulacion fungicida.Info
- Publication number
- ES2201635T3 ES2201635T3 ES99302964T ES99302964T ES2201635T3 ES 2201635 T3 ES2201635 T3 ES 2201635T3 ES 99302964 T ES99302964 T ES 99302964T ES 99302964 T ES99302964 T ES 99302964T ES 2201635 T3 ES2201635 T3 ES 2201635T3
- Authority
- ES
- Spain
- Prior art keywords
- weight
- water
- composition according
- agent
- formula
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
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- 230000000855 fungicidal effect Effects 0.000 title claims abstract description 39
- 239000000417 fungicide Substances 0.000 title abstract description 14
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- GNVDAZSPJWCIQZ-UHFFFAOYSA-N flusulfamide Chemical compound ClC1=CC([N+](=O)[O-])=CC=C1NS(=O)(=O)C1=CC=C(Cl)C(C(F)(F)F)=C1 GNVDAZSPJWCIQZ-UHFFFAOYSA-N 0.000 description 1
- PTCGDEVVHUXTMP-UHFFFAOYSA-N flutolanil Chemical compound CC(C)OC1=CC=CC(NC(=O)C=2C(=CC=CC=2)C(F)(F)F)=C1 PTCGDEVVHUXTMP-UHFFFAOYSA-N 0.000 description 1
- HKIOYBQGHSTUDB-UHFFFAOYSA-N folpet Chemical compound C1=CC=C2C(=O)N(SC(Cl)(Cl)Cl)C(=O)C2=C1 HKIOYBQGHSTUDB-UHFFFAOYSA-N 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- ZEYJIQLVKGBLEM-UHFFFAOYSA-N fuberidazole Chemical compound C1=COC(C=2N=C3[CH]C=CC=C3N=2)=C1 ZEYJIQLVKGBLEM-UHFFFAOYSA-N 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 125000001188 haloalkyl group Chemical group 0.000 description 1
- 230000002363 herbicidal effect Effects 0.000 description 1
- 239000004009 herbicide Substances 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
- 229940071870 hydroiodic acid Drugs 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- QTYCMDBMOLSEAM-UHFFFAOYSA-N ipconazole Chemical compound C1=NC=NN1CC1(O)C(C(C)C)CCC1CC1=CC=C(Cl)C=C1 QTYCMDBMOLSEAM-UHFFFAOYSA-N 0.000 description 1
- FCOAHACKGGIURQ-UHFFFAOYSA-N iprobenfos Chemical compound CC(C)OP(=O)(OC(C)C)SCC1=CC=CC=C1 FCOAHACKGGIURQ-UHFFFAOYSA-N 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- WPOOICLZIIBUBM-UHFFFAOYSA-H iron;iron(3+);methyl-dioxido-oxo-$l^{5}-arsane Chemical compound [Fe].[Fe+3].[Fe+3].C[As]([O-])([O-])=O.C[As]([O-])([O-])=O.C[As]([O-])([O-])=O WPOOICLZIIBUBM-UHFFFAOYSA-H 0.000 description 1
- UFHLMYOGRXOCSL-UHFFFAOYSA-N isoprothiolane Chemical compound CC(C)OC(=O)C(C(=O)OC(C)C)=C1SCCS1 UFHLMYOGRXOCSL-UHFFFAOYSA-N 0.000 description 1
- PVTHJAPFENJVNC-MHRBZPPQSA-N kasugamycin Chemical compound N[C@H]1C[C@H](NC(=N)C(O)=O)[C@@H](C)O[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@H](O)[C@@H]1O PVTHJAPFENJVNC-MHRBZPPQSA-N 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 239000008101 lactose Substances 0.000 description 1
- 235000014666 liquid concentrate Nutrition 0.000 description 1
- 239000011344 liquid material Substances 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- YKSNLCVSTHTHJA-UHFFFAOYSA-L maneb Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S YKSNLCVSTHTHJA-UHFFFAOYSA-L 0.000 description 1
- 229920000940 maneb Polymers 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- CIFWZNRJIBNXRE-UHFFFAOYSA-N mepanipyrim Chemical compound CC#CC1=CC(C)=NC(NC=2C=CC=CC=2)=N1 CIFWZNRJIBNXRE-UHFFFAOYSA-N 0.000 description 1
- BCTQJXQXJVLSIG-UHFFFAOYSA-N mepronil Chemical compound CC(C)OC1=CC=CC(NC(=O)C=2C(=CC=CC=2)C)=C1 BCTQJXQXJVLSIG-UHFFFAOYSA-N 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- ZWJNEYVWPYIKMB-UHFFFAOYSA-N methfuroxam Chemical compound CC1=C(C)OC(C)=C1C(=O)NC1=CC=CC=C1 ZWJNEYVWPYIKMB-UHFFFAOYSA-N 0.000 description 1
- ZQEIXNIJLIKNTD-UHFFFAOYSA-N methyl N-(2,6-dimethylphenyl)-N-(methoxyacetyl)alaninate Chemical compound COCC(=O)N(C(C)C(=O)OC)C1=C(C)C=CC=C1C ZQEIXNIJLIKNTD-UHFFFAOYSA-N 0.000 description 1
- CJPQIRJHIZUAQP-UHFFFAOYSA-N methyl N-(2,6-dimethylphenyl)-N-(phenylacetyl)alaninate Chemical compound CC=1C=CC=C(C)C=1N(C(C)C(=O)OC)C(=O)CC1=CC=CC=C1 CJPQIRJHIZUAQP-UHFFFAOYSA-N 0.000 description 1
- CIEXPHRYOLIQQD-UHFFFAOYSA-N methyl N-(2,6-dimethylphenyl)-N-2-furoylalaninate Chemical compound CC=1C=CC=C(C)C=1N(C(C)C(=O)OC)C(=O)C1=CC=CO1 CIEXPHRYOLIQQD-UHFFFAOYSA-N 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- WBYWAXJHAXSJNI-UHFFFAOYSA-N methyl p-hydroxycinnamate Natural products OC(=O)C=CC1=CC=CC=C1 WBYWAXJHAXSJNI-UHFFFAOYSA-N 0.000 description 1
- 230000003020 moisturizing effect Effects 0.000 description 1
- BLCKKNLGFULNRC-UHFFFAOYSA-L n,n-dimethylcarbamodithioate;nickel(2+) Chemical compound [Ni+2].CN(C)C([S-])=S.CN(C)C([S-])=S BLCKKNLGFULNRC-UHFFFAOYSA-L 0.000 description 1
- PZYDAVFRVJXFHS-UHFFFAOYSA-N n-cyclohexyl-2-pyrrolidone Chemical compound O=C1CCCN1C1CCCCC1 PZYDAVFRVJXFHS-UHFFFAOYSA-N 0.000 description 1
- 229910001453 nickel ion Inorganic materials 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- UWVQIROCRJWDKL-UHFFFAOYSA-N oxadixyl Chemical compound CC=1C=CC=C(C)C=1N(C(=O)COC)N1CCOC1=O UWVQIROCRJWDKL-UHFFFAOYSA-N 0.000 description 1
- AMEKQAFGQBKLKX-UHFFFAOYSA-N oxycarboxin Chemical compound O=S1(=O)CCOC(C)=C1C(=O)NC1=CC=CC=C1 AMEKQAFGQBKLKX-UHFFFAOYSA-N 0.000 description 1
- 239000011049 pearl Substances 0.000 description 1
- OGYFATSSENRIKG-UHFFFAOYSA-N pencycuron Chemical compound C1=CC(Cl)=CC=C1CN(C(=O)NC=1C=CC=CC=1)C1CCCC1 OGYFATSSENRIKG-UHFFFAOYSA-N 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- WHHIPMZEDGBUCC-UHFFFAOYSA-N probenazole Chemical compound C1=CC=C2C(OCC=C)=NS(=O)(=O)C2=C1 WHHIPMZEDGBUCC-UHFFFAOYSA-N 0.000 description 1
- TVLSRXXIMLFWEO-UHFFFAOYSA-N prochloraz Chemical compound C1=CN=CN1C(=O)N(CCC)CCOC1=C(Cl)C=C(Cl)C=C1Cl TVLSRXXIMLFWEO-UHFFFAOYSA-N 0.000 description 1
- WZZLDXDUQPOXNW-UHFFFAOYSA-N propamocarb Chemical compound CCCOC(=O)NCCCN(C)C WZZLDXDUQPOXNW-UHFFFAOYSA-N 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- STJLVHWMYQXCPB-UHFFFAOYSA-N propiconazole Chemical compound O1C(CCC)COC1(C=1C(=CC(Cl)=CC=1)Cl)CN1N=CN=C1 STJLVHWMYQXCPB-UHFFFAOYSA-N 0.000 description 1
- KKMLIVYBGSAJPM-UHFFFAOYSA-L propineb Chemical compound [Zn+2].[S-]C(=S)NC(C)CNC([S-])=S KKMLIVYBGSAJPM-UHFFFAOYSA-L 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- JOOMJVFZQRQWKR-UHFFFAOYSA-N pyrazophos Chemical compound N1=C(C)C(C(=O)OCC)=CN2N=C(OP(=S)(OCC)OCC)C=C21 JOOMJVFZQRQWKR-UHFFFAOYSA-N 0.000 description 1
- ZLIBICFPKPWGIZ-UHFFFAOYSA-N pyrimethanil Chemical compound CC1=CC(C)=NC(NC=2C=CC=CC=2)=N1 ZLIBICFPKPWGIZ-UHFFFAOYSA-N 0.000 description 1
- XRJLAOUDSILTFT-UHFFFAOYSA-N pyroquilon Chemical compound O=C1CCC2=CC=CC3=C2N1CC3 XRJLAOUDSILTFT-UHFFFAOYSA-N 0.000 description 1
- FBQQHUGEACOBDN-UHFFFAOYSA-N quinomethionate Chemical compound N1=C2SC(=O)SC2=NC2=CC(C)=CC=C21 FBQQHUGEACOBDN-UHFFFAOYSA-N 0.000 description 1
- WRPIRSINYZBGPK-UHFFFAOYSA-N quinoxyfen Chemical compound C1=CC(F)=CC=C1OC1=CC=NC2=CC(Cl)=CC(Cl)=C12 WRPIRSINYZBGPK-UHFFFAOYSA-N 0.000 description 1
- 239000013049 sediment Substances 0.000 description 1
- 230000003381 solubilizing effect Effects 0.000 description 1
- PUYXTUJWRLOUCW-UHFFFAOYSA-N spiroxamine Chemical compound O1C(CN(CC)CCC)COC11CCC(C(C)(C)C)CC1 PUYXTUJWRLOUCW-UHFFFAOYSA-N 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 229960005322 streptomycin Drugs 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
- 230000009885 systemic effect Effects 0.000 description 1
- ROZUQUDEWZIBHV-UHFFFAOYSA-N tecloftalam Chemical compound OC(=O)C1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1C(=O)NC1=CC=CC(Cl)=C1Cl ROZUQUDEWZIBHV-UHFFFAOYSA-N 0.000 description 1
- XQTLDIFVVHJORV-UHFFFAOYSA-N tecnazene Chemical compound [O-][N+](=O)C1=C(Cl)C(Cl)=CC(Cl)=C1Cl XQTLDIFVVHJORV-UHFFFAOYSA-N 0.000 description 1
- 239000004308 thiabendazole Substances 0.000 description 1
- WJCNZQLZVWNLKY-UHFFFAOYSA-N thiabendazole Chemical compound S1C=NC(C=2NC3=CC=CC=C3N=2)=C1 WJCNZQLZVWNLKY-UHFFFAOYSA-N 0.000 description 1
- 235000010296 thiabendazole Nutrition 0.000 description 1
- 229960004546 thiabendazole Drugs 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- WOSNCVAPUOFXEH-UHFFFAOYSA-N thifluzamide Chemical compound S1C(C)=NC(C(F)(F)F)=C1C(=O)NC1=C(Br)C=C(OC(F)(F)F)C=C1Br WOSNCVAPUOFXEH-UHFFFAOYSA-N 0.000 description 1
- QGHREAKMXXNCOA-UHFFFAOYSA-N thiophanate-methyl Chemical compound COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC QGHREAKMXXNCOA-UHFFFAOYSA-N 0.000 description 1
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 1
- 229960002447 thiram Drugs 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- OBZIQQJJIKNWNO-UHFFFAOYSA-N tolclofos-methyl Chemical group COP(=S)(OC)OC1=C(Cl)C=C(C)C=C1Cl OBZIQQJJIKNWNO-UHFFFAOYSA-N 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
- BAZVSMNPJJMILC-UHFFFAOYSA-N triadimenol Chemical compound C1=NC=NN1C(C(O)C(C)(C)C)OC1=CC=C(Cl)C=C1 BAZVSMNPJJMILC-UHFFFAOYSA-N 0.000 description 1
- IQGKIPDJXCAMSM-UHFFFAOYSA-N triazoxide Chemical compound N=1C2=CC=C(Cl)C=C2[N+]([O-])=NC=1N1C=CN=C1 IQGKIPDJXCAMSM-UHFFFAOYSA-N 0.000 description 1
- YNJBWRMUSHSURL-UHFFFAOYSA-N trichloroacetic acid Chemical compound OC(=O)C(Cl)(Cl)Cl YNJBWRMUSHSURL-UHFFFAOYSA-N 0.000 description 1
- DQJCHOQLCLEDLL-UHFFFAOYSA-N tricyclazole Chemical compound CC1=CC=CC2=C1N1C=NN=C1S2 DQJCHOQLCLEDLL-UHFFFAOYSA-N 0.000 description 1
- HSMVPDGQOIQYSR-KGENOOAVSA-N triflumizole Chemical compound C1=CN=CN1C(/COCCC)=N/C1=CC=C(Cl)C=C1C(F)(F)F HSMVPDGQOIQYSR-KGENOOAVSA-N 0.000 description 1
- RROQIUMZODEXOR-UHFFFAOYSA-N triforine Chemical compound O=CNC(C(Cl)(Cl)Cl)N1CCN(C(NC=O)C(Cl)(Cl)Cl)CC1 RROQIUMZODEXOR-UHFFFAOYSA-N 0.000 description 1
- JARYYMUOCXVXNK-CSLFJTBJSA-N validamycin A Chemical compound N([C@H]1C[C@@H]([C@H]([C@H](O)[C@H]1O)O[C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)CO)[C@H]1C=C(CO)[C@@H](O)[C@H](O)[C@H]1O JARYYMUOCXVXNK-CSLFJTBJSA-N 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- DUBNHZYBDBBJHD-UHFFFAOYSA-L ziram Chemical compound [Zn+2].CN(C)C([S-])=S.CN(C)C([S-])=S DUBNHZYBDBBJHD-UHFFFAOYSA-L 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/647—Triazoles; Hydrogenated triazoles
- A01N43/653—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US09/063,199 US6096769A (en) | 1998-04-20 | 1998-04-20 | Fungicidal co-formulation |
| US63199 | 1998-04-20 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2201635T3 true ES2201635T3 (es) | 2004-03-16 |
Family
ID=22047628
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES99302964T Expired - Lifetime ES2201635T3 (es) | 1998-04-20 | 1999-04-16 | Co-formulacion fungicida. |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US6096769A (de) |
| EP (1) | EP0951831B1 (de) |
| JP (1) | JP2000001407A (de) |
| AR (1) | AR019082A1 (de) |
| AT (1) | ATE242599T1 (de) |
| BR (1) | BR9901100B1 (de) |
| CA (3) | CA2691601C (de) |
| DE (1) | DE69908701T2 (de) |
| DK (1) | DK0951831T3 (de) |
| ES (1) | ES2201635T3 (de) |
| PT (1) | PT951831E (de) |
| RU (1) | RU2242124C2 (de) |
| UA (1) | UA65545C2 (de) |
Families Citing this family (27)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DK1023832T3 (da) * | 1999-01-29 | 2005-02-21 | Basf Ag | Vandigt suspensionskoncentrat |
| WO2000045636A1 (en) * | 1999-02-08 | 2000-08-10 | Cognis Corporation | Pigmented coatings exhibiting reduced fading |
| GB0021786D0 (en) * | 2000-09-05 | 2000-10-18 | Zeneca Ltd | Fungicidal formulations |
| ITMI20012430A1 (it) * | 2001-11-19 | 2003-05-19 | Isagro Spa | Composizioni a base di sali rameici sali rameici e loro utilizzo per il controllo di fitopatogeni |
| CA2477000C (en) * | 2002-03-01 | 2012-05-08 | Basf Aktiengesellschaft | Fungicidal mixtures based on prothioconazole and a strobilurin derivative |
| EP1611789B1 (de) * | 2002-07-10 | 2007-10-17 | Basf Aktiengesellschaft | Fungizide Mischungen auf Basis von Dithianon |
| EP2345329B1 (de) * | 2003-04-09 | 2019-09-18 | Koppers Performance Chemicals Inc. | Mikronisierte formulierungen zur holzkonservierung |
| US8637089B2 (en) * | 2003-04-09 | 2014-01-28 | Osmose, Inc. | Micronized wood preservative formulations |
| ATE495669T1 (de) * | 2004-07-16 | 2011-02-15 | Ishihara Sangyo Kaisha | Bakterizide zusammensetzung für landwirtschaft oder gartenbau sowie verfahren zur bekämpfung von pflanzenkrankheiten |
| JP4743831B2 (ja) * | 2004-11-17 | 2011-08-10 | 北興化学工業株式会社 | 液状農薬製剤 |
| NZ583584A (en) * | 2005-09-29 | 2010-05-28 | Janssen Pharmaceutica Nv | Synergistic antifungal combinations of imazalil and fosetyl-Al (aluminum tris(ethyl phosphite)) |
| WO2007045455A1 (en) * | 2005-10-20 | 2007-04-26 | Syngenta Participations Ag | Fungicidal compositions |
| DE102006026106A1 (de) * | 2006-05-11 | 2007-11-15 | Isp Biochema Schwaben Gmbh | Flüssiges Konzentrat für die Filmkonservierung |
| CA2682922A1 (en) * | 2007-04-25 | 2008-11-06 | Basf Se | Fungicide mixtures |
| EP3150068B1 (de) | 2007-08-16 | 2019-10-09 | Basf Se | Samenbehandlungszusammensetzungen und -verfahren |
| CN101959413A (zh) * | 2008-02-28 | 2011-01-26 | 先正达参股股份有限公司 | 农药组合 |
| TWI524844B (zh) | 2008-05-12 | 2016-03-11 | 先正達合夥公司 | 除害組成物 |
| UA101382C2 (ru) | 2008-07-04 | 2013-03-25 | Басф Се | Фунгицидные смеси, содержащие замещенные 1-метилпиразол-4-илкарбоксанилиды |
| RU2373711C1 (ru) * | 2008-08-20 | 2009-11-27 | Закрытое Акионерное Общество Фирма "Август" | Фунгицидная композиция и способ борьбы с фитопатогенными грибами |
| CN103596934B (zh) | 2011-05-31 | 2015-08-19 | 株式会社吴羽 | 三氮杂茂化合物、及其运用 |
| EP2719281A4 (de) * | 2011-06-07 | 2014-11-19 | Kureha Corp | Landwirtschaftliche oder gartenbauliche chemikalien, zusammensetzung zur bekämpfung von pflanzenkrankheiten, verfahren zur bekämpfung von pflanzenkrankheiten und produkt zur bekämpfung von pflanzenkrankheiten |
| WO2013026470A1 (en) * | 2011-08-22 | 2013-02-28 | Agriphar S.A. | Aqueous suspension concentrate comprising dodecylguanidine |
| WO2015083436A1 (ja) | 2013-12-05 | 2015-06-11 | 株式会社クレハ | 農園芸用薬剤、植物病害防除方法および植物病害防除用製品 |
| EP3078265B1 (de) * | 2013-12-05 | 2017-06-07 | Kureha Corporation | Landwirtschaftliche und gärtnerische präparate, verfahren zur bekämpfung von pflanzenkrankheiten und produkt zur bekämpfung von pflanzenkrankheiten |
| CN104756999A (zh) * | 2015-03-23 | 2015-07-08 | 陕西西大华特科技实业有限公司 | 一种含叶菌唑和噻霉酮的杀菌组合物及应用 |
| CN106900720A (zh) * | 2017-04-27 | 2017-06-30 | 上海赫腾精细化工有限公司 | 一种叶菌唑与百菌清的复配杀菌剂组合物及其应用 |
| AU2020317060B2 (en) * | 2019-07-24 | 2021-10-07 | Elders Toll Formulation Pty Ltd | Fungicide composition |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0625140B2 (ja) * | 1986-11-10 | 1994-04-06 | 呉羽化学工業株式会社 | 新規アゾール誘導体、その製造方法及び該誘導体の農園芸用薬剤 |
| GB8710105D0 (en) * | 1987-04-29 | 1987-06-03 | Ici Plc | Pesticidal formulations |
| DE4001115A1 (de) * | 1990-01-17 | 1991-07-18 | Bayer Ag | Fungizide wirkstoffkombinationen |
| FR2663195A1 (fr) * | 1990-06-13 | 1991-12-20 | Rhone Poulenc Agrochimie | Procede de traitement fongicide foliaire au moyen d'un triazole et composition fongicide pour mettre en óoeuvre le procede. |
| GB9116557D0 (en) * | 1991-07-31 | 1991-09-11 | Shell Int Research | Fungicidal compositions |
| DE4130298A1 (de) * | 1991-09-12 | 1993-03-18 | Basf Ag | Fungizide mischungen |
| USH1400H (en) * | 1992-08-11 | 1995-01-03 | Culbreath; Albert K. | Fungicide |
| GB9320744D0 (en) * | 1992-11-04 | 1993-12-01 | Zeneca Ltd | Oxa and thiadiazole derivatives |
| GB9307247D0 (en) * | 1993-04-07 | 1993-06-02 | Zeneca Ltd | Fungicidal compounds |
| AU1280095A (en) * | 1993-12-27 | 1995-07-17 | Sumitomo Chemical Company, Limited | Bactericidal composition |
| GB9413980D0 (en) * | 1994-07-12 | 1994-08-31 | Rohm & Haas France | Novel agrochemical formulation |
| DE19636686A1 (de) * | 1996-09-10 | 1998-03-12 | Basf Ag | Fungizide Mischungen |
-
1998
- 1998-04-20 US US09/063,199 patent/US6096769A/en not_active Expired - Lifetime
-
1999
- 1999-04-12 CA CA2691601A patent/CA2691601C/en not_active Expired - Fee Related
- 1999-04-12 BR BRPI9901100-0B1A patent/BR9901100B1/pt not_active IP Right Cessation
- 1999-04-12 CA CA2691758A patent/CA2691758C/en not_active Expired - Fee Related
- 1999-04-12 JP JP11104264A patent/JP2000001407A/ja active Pending
- 1999-04-12 CA CA2268619A patent/CA2268619C/en not_active Expired - Fee Related
- 1999-04-16 DE DE69908701T patent/DE69908701T2/de not_active Expired - Lifetime
- 1999-04-16 ES ES99302964T patent/ES2201635T3/es not_active Expired - Lifetime
- 1999-04-16 EP EP99302964A patent/EP0951831B1/de not_active Expired - Lifetime
- 1999-04-16 PT PT99302964T patent/PT951831E/pt unknown
- 1999-04-16 UA UA99042157A patent/UA65545C2/uk unknown
- 1999-04-16 AT AT99302964T patent/ATE242599T1/de active
- 1999-04-16 DK DK99302964T patent/DK0951831T3/da active
- 1999-04-19 RU RU99108250/04A patent/RU2242124C2/ru not_active IP Right Cessation
- 1999-04-19 AR ARP990101805A patent/AR019082A1/es active IP Right Grant
Also Published As
| Publication number | Publication date |
|---|---|
| EP0951831B1 (de) | 2003-06-11 |
| BR9901100B1 (pt) | 2013-06-18 |
| DE69908701D1 (de) | 2003-07-17 |
| US6096769A (en) | 2000-08-01 |
| BR9901100A (pt) | 2000-03-21 |
| DE69908701T2 (de) | 2004-04-29 |
| DK0951831T3 (da) | 2003-07-14 |
| ATE242599T1 (de) | 2003-06-15 |
| CA2691601C (en) | 2012-10-02 |
| CA2268619C (en) | 2010-09-14 |
| EP0951831A1 (de) | 1999-10-27 |
| CA2691758A1 (en) | 1999-10-20 |
| AR019082A1 (es) | 2001-12-26 |
| RU2242124C2 (ru) | 2004-12-20 |
| CA2691758C (en) | 2012-06-05 |
| CA2268619A1 (en) | 1999-10-20 |
| PT951831E (pt) | 2003-10-31 |
| JP2000001407A (ja) | 2000-01-07 |
| CA2691601A1 (en) | 1999-10-20 |
| UA65545C2 (en) | 2004-04-15 |
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